FDA UDI In Commercial Distribution 🇺🇸 United States

Zemits DuoCratus

DI: 00860010841174 · Model: 1 · Advance-Esthetic LLC
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zemits DuoCratus
Primary DI
00860010841174
Version / Model
1
Catalog Number
111921
Company Name
Advance-Esthetic LLC
Labeler DUNS
043911204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-06
Public Version
1
Public Version Date
2024-02-14
Public Version Status
New
Public Device Record Key
7a6cf6d6-eb2d-470f-b7c6-87e7a67eeb25

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system
58786 Dermatological diode laser system

Identifiers

Type ID
Primary 00860010841174

Customer Contacts

Phone
8889993996